European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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01 1ZAKŁADY FARMACEUTYCZNE POLPHARMA S.A. Starogard Gdański PL
02 1TAPI NL B.V. Amsterdam NL
03 1EMCURE PHARMACEUTICALS LIMITED Pune IN
04 1HETERO LABS LIMITED Hyderabad IN
05 1HIKMA PHARMACEUTICALS LLC Amman JO
06 1JUBILANT BIOSYS LIMITED Nanjangud IN
07 1SCINOPHARM TAIWAN, LTD. Shan-Hua TW
08 1SHANDONG NEW TIME PHARMACEUTICAL CO., LTD. Linyi CN
09 1SHILPA PHARMA LIFESCIENCES LIMITED Raichur IN
10 1USV PRIVATE LIMITED Mumbai IN
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01 10Zoledronic acid monohydrate
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01 1China
02 6India
03 1Israel
04 1Poland
05 1Taiwan
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01 10Valid
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Certificate Number : CEP 2018-191 - Rev 03
Status : Valid
Issue Date : 2024-07-23
Type : Chemical
Substance Number : 2743
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : CEP 2020-018 - Rev 02
Status : Valid
Issue Date : 2025-02-28
Type : Chemical
Substance Number : 2743
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Certificate Number : CEP 2020-205 - Rev 03
Status : Valid
Issue Date : 2024-09-03
Type : Chemical
Substance Number : 2743

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Certificate Number : CEP 2021-181 - Rev 00
Status : Valid
Issue Date : 2023-10-27
Type : Chemical
Substance Number : 2743

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Certificate Number : CEP 2023-275 - Rev 00
Status : Valid
Issue Date : 2024-12-13
Type : Chemical
Substance Number : 2743

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Certificate Number : CEP 2019-349 - Rev 02
Status : Valid
Issue Date : 2025-09-04
Type : Chemical
Substance Number : 2743

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Certificate Number : R0-CEP 2021-177 - Rev 00
Status : Valid
Issue Date : 2022-08-26
Type : Chemical
Substance Number : 2743

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Certificate Number : CEP 2019-281 - Rev 01
Status : Valid
Issue Date : 2024-10-16
Type : Chemical
Substance Number : 2743

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Certificate Number : CEP 2021-269 - Rev 01
Status : Valid
Issue Date : 2024-10-04
Type : Chemical
Substance Number : 2743

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Certificate Number : R0-CEP 2022-203 - Rev 00
Status : Valid
Issue Date : 2023-02-10
Type : Chemical
Substance Number : 2743

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PharmaCompass offers a list of Zoledronic Acid API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Zoledronic Acid manufacturer or Zoledronic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zoledronic Acid manufacturer or Zoledronic Acid supplier.
PharmaCompass also assists you with knowing the Zoledronic Acid API Price utilized in the formulation of products. Zoledronic Acid API Price is not always fixed or binding as the Zoledronic Acid Price is obtained through a variety of data sources. The Zoledronic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aclasta and Reclast manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aclasta and Reclast, including repackagers and relabelers. The FDA regulates Aclasta and Reclast manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aclasta and Reclast API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Aclasta and Reclast manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aclasta and Reclast supplier is an individual or a company that provides Aclasta and Reclast active pharmaceutical ingredient (API) or Aclasta and Reclast finished formulations upon request. The Aclasta and Reclast suppliers may include Aclasta and Reclast API manufacturers, exporters, distributors and traders.
click here to find a list of Aclasta and Reclast suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Aclasta and Reclast CEP of the European Pharmacopoeia monograph is often referred to as a Aclasta and Reclast Certificate of Suitability (COS). The purpose of a Aclasta and Reclast CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aclasta and Reclast EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aclasta and Reclast to their clients by showing that a Aclasta and Reclast CEP has been issued for it. The manufacturer submits a Aclasta and Reclast CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aclasta and Reclast CEP holder for the record. Additionally, the data presented in the Aclasta and Reclast CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aclasta and Reclast DMF.
A Aclasta and Reclast CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aclasta and Reclast CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Aclasta and Reclast suppliers with CEP (COS) on PharmaCompass.
We have 10 companies offering Aclasta and Reclast
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